Horie M - Search Results

1

Improved Risk Stratification of Patients With Brugada Syndrome by the New Japanese Circulation Society Guideline　- A Multicenter Validation Study.

Wakamiya A, Kamakura T, Shinohara T, Yodogawa K, Murakoshi N, Morita H, Takahashi N, Inden Y, Shimizu W, Nogami A, Horie M, Nakajima K, Kataoka N, Wada M, Yamagata K, Ishibashi K, Inoue Y, Miyamoto K, Nagase S, Noda T, Aiba T, Yasuda S, Ieda M, Kusano K. Wakamiya A, et al. Among authors: horie m. Circ J. 2020 Nov 25;84(12):2158-2165. doi: 10.1253/circj.CJ-19-0910. Epub 2020 Oct 17. Circ J. 2020. PMID: 33071242 Free article.

2

Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1.

Kubota T, Shimizu W, Kamakura S, Horie M. Kubota T, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 2000 Sep;11(9):1048-54. doi: 10.1111/j.1540-8167.2000.tb00178.x. J Cardiovasc Electrophysiol. 2000. PMID: 11021476

3

Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome.

Noda T, Takaki H, Kurita T, Suyama K, Nagaya N, Taguchi A, Aihara N, Kamakura S, Sunagawa K, Nakamura K, Ohe T, Horie M, Napolitano C, Towbin JA, Priori SG, Shimizu W. Noda T, et al. Among authors: horie m. Eur Heart J. 2002 Jun;23(12):975-83. doi: 10.1053/euhj.2001.3079. Eur Heart J. 2002. PMID: 12069453

4

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.

Takenaka K, Ai T, Shimizu W, Kobori A, Ninomiya T, Otani H, Kubota T, Takaki H, Kamakura S, Horie M. Takenaka K, et al. Among authors: horie m. Circulation. 2003 Feb 18;107(6):838-44. doi: 10.1161/01.cir.0000048142.85076.a2. Circulation. 2003. PMID: 12591753 Clinical Trial.

5

Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.

Kobori A, Sarai N, Shimizu W, Nakamura Y, Murakami Y, Makiyama T, Ohno S, Takenaka K, Ninomiya T, Fujiwara Y, Matsuoka S, Takano M, Noma A, Kita T, Horie M. Kobori A, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 2004 Feb;15(2):190-9. doi: 10.1046/j.1540-8167.2004.03212.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028050

6

Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.

Shimizu W, Horie M, Ohno S, Takenaka K, Yamaguchi M, Shimizu M, Washizuka T, Aizawa Y, Nakamura K, Ohe T, Aiba T, Miyamoto Y, Yoshimasa Y, Towbin JA, Priori SG, Kamakura S. Shimizu W, et al. Among authors: horie m. J Am Coll Cardiol. 2004 Jul 7;44(1):117-25. doi: 10.1016/j.jacc.2004.03.043. J Am Coll Cardiol. 2004. PMID: 15234419 Free article.

7

Cellular and ionic mechanism for drug-induced long QT syndrome and effectiveness of verapamil.

Aiba T, Shimizu W, Inagaki M, Noda T, Miyoshi S, Ding WG, Zankov DP, Toyoda F, Matsuura H, Horie M, Sunagawa K. Aiba T, et al. Among authors: horie m. J Am Coll Cardiol. 2005 Jan 18;45(2):300-7. doi: 10.1016/j.jacc.2004.09.069. J Am Coll Cardiol. 2005. PMID: 15653031 Free article.

8

The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

Crotti L, Spazzolini C, Schwartz PJ, Shimizu W, Denjoy I, Schulze-Bahr E, Zaklyazminskaya EV, Swan H, Ackerman MJ, Moss AJ, Wilde AA, Horie M, Brink PA, Insolia R, De Ferrari GM, Crimi G. Crotti L, et al. Among authors: horie m. Circulation. 2007 Nov 20;116(21):2366-75. doi: 10.1161/CIRCULATIONAHA.107.726950. Epub 2007 Nov 5. Circulation. 2007. PMID: 17984373

9

Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.

Sakaguchi T, Shimizu W, Itoh H, Noda T, Miyamoto Y, Nagaoka I, Oka Y, Ashihara T, Ito M, Tsuji K, Ohno S, Makiyama T, Kamakura S, Horie M. Sakaguchi T, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 2008 Aug;19(8):794-9. doi: 10.1111/j.1540-8167.2008.01138.x. Epub 2008 Mar 26. J Cardiovasc Electrophysiol. 2008. PMID: 18373596

10

A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.

Ohno S, Kubota T, Yoshida H, Tsuji K, Makiyama T, Yamada S, Kuga K, Yamaguchi I, Kita T, Horie M. Ohno S, et al. Among authors: horie m. Circ J. 2008 May;72(5):687-93. doi: 10.1253/circj.72.687. Circ J. 2008. PMID: 18441444 Free article.

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